- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04789967
Effects of Imagery Therapy vs Progressive Muscle Relaxation Therapy on Patients With Functional Abdominal Bloating
November 4, 2022 updated by: Vincent Tee Wei Shen, Universiti Sains Malaysia
The Effects of Imagery Treatments vs Progressive Muscle Relaxation Therapy in Terms of Clinical, Psychological and Physiological Aspects Among Patients With Functional Abdominal Bloating
65% of the general population reported experiencing moderate to severe bloating symptoms.
Bloating could be disturbing to patients and frustrating to the physicians as an effective treatment is still lacking.
Guided Imagery (GI) involves the structured visualisation of mental images with somatic sensory; whereas Progressive Muscle Relaxation (PMR) focuses on tightening and relaxing the body's specific muscle groups.
The development and validation of GI or PMR interventions to treat patients with functional abdominal bloating are relatively novel.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The baseline variables of the patient would be obtained at the outpatient Gastrointestinal Medical clinic.
A thorough general clinical interview that encompasses medical and psychological history, discussion of the nature and severity of the current symptoms, and review of past treatments and conclusions of any medical evaluation and tests.
This is to make sure that the patients have been comprehensively evaluated medically and to rule out other causes of abdominal bloating before reaching a firm diagnosis of functional abdominal bloating as suggested in ROME IV Criteria.
Questionnaires will be given out and patients were asked to fill it up on the spot.
Electrical activity and abdominal circumference would be measured at an enclosed space with appropriate privacy and accompanied by a chaperone.
Study Type
Interventional
Enrollment (Actual)
96
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Kelantan
-
Kubang Kerian, Kelantan, Malaysia, 16150
- Universiti Sains Malaysia
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Participants with abdominal bloating as determined using the Malay version Rome III criteria which was validated and translated by past researchers (Lee et al, 2012) and/or patients who were suggested by clinicians.
- Participants must be 18 years and above, and of either gender.
- Participants are able to read, write, or understand the Malay language.
Exclusion Criteria:
- Patients with abdominal bloating due to organic disorder
- Patients with recent abdominal surgeries (within 3 months) or previous major abdominal surgeries
- Patients with major neurological and psychological disorders including stroke, schizophrenia, major depression.
- Patients with medical history which may be the red flag for other FGIDs and organic disorders .
- Patients who are on psychotropic medications or psychotherapy which may confound outcome of imagery of sham intervention.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Guided Imagery (GI)
A 8 minute audio that focuses on evoking mental images in reducing the abdominal bloating sensation in patients
|
Individualized Guided Imagery (GI) technique, an alternative type of relaxation therapy.
The content of GI usually includes scenery, places or any image projected to the mind.
By using information generated, participants are guided to create a place in their mind using their senses of touch, sound, smell, sight and taste.
Other Names:
|
|
Active Comparator: Progressive Muscle Relaxation (PMR)
A 8 minute audio that focuses on contracting certain muscle groups and relaxing it progressively in reducing the abdominal bloating sensation in patients
|
Progressive muscle relaxation (PMR) therapy works by progressively relaxing and tensing the muscle groups throughout the entire body.
Each muscle group will be tensed for about 5 seconds.
If there's any pain or discomfort at any of the targeted areas, participants were told to omit that particular step.
Constant purposeful deep breathing was instructed throughout the session especially in between changes of muscle.
Other Names:
|
|
Placebo Comparator: Audiobook
A 8 minute audio that focuses on providing educational information regarding functional gastrointestinal disorders and related knowledge.
|
Participants in the control group will receive an audiobook that targets to educate patients regarding gut-brain disorders, functional gastrointestinal disorders, causes of functional abdominal bloating, and treatment modalities available.
Relaxing musical background will be added to facilitate the delivery.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Symptoms severity
Time Frame: 1 month
|
Measured using the Malay version of Bloating Severity Questionnaire (BSQ-M).
It consists of two components: five-item Sev24 and seven-item SevGen.
The responses were in a multiple-choice answer format on different degrees of effect towards individuals on the basis of intensity, frequency and severity (less severe to more severe; range 1 to 4,5,6,7 or 8 varied by items).
Higher scores in BSQ indicate worse severity.
|
1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health belief
Time Frame: 1 month
|
Measured using the Malay-Language Health of Bloating (HB-Bloat) Scale.
The questionnaire consists of 12 items and 3 domains: attitude (3 items), subjective norm (5 items), perceived control towards self-management (4 items).
All responses were measured on a five-point Likert scale from 1 (strongly disagree) to 5 (strongly agree).
|
1 month
|
|
Health seeking Intention
Time Frame: 1 month
|
Measured using Health Seeking Intention for Abdominal Bloating Scale.
It is a 5 point Likert scale that consists of 1 domain and 1 item. 1 indicates "strongly diagree" while 5 indicates "strongly agree"
|
1 month
|
|
Health promoting behavior
Time Frame: 1 month
|
Measured using Health Promoting Behavior Scale of Abdominal Bloating.
The questionnaire consists of 4 domains and 15 items.
The questionnaire is a 5 point Likert scales, whereby 1 is considered strongly disagree and 5 is considered strongly agree.
|
1 month
|
|
Anxiety
Time Frame: 1 month
|
Measured using the Malay version of Hospital Anxiety and Depression Scale (HADS).
It comprises of 14 items, seven of which is related to anxiety symptoms.
Each item is coded from 0 to 3. The scores for anxiety and depression can therefore vary from 0 to 21, depending on the presence and severity of the symptoms.
A score between 0 and 7 does not indicate the presence of the symptoms of anxiety; a score between 8 and 10 indicates the presence of a moderate symptom; a score of 11 and above indicates a significant number of symptoms of anxiety corresponding to confirmed cases.
|
1 month
|
|
Depression
Time Frame: 1 month
|
Measured using the Malay version of Hospital Anxiety and Depression Scale (HADS).
It comprises of 14 items, seven of which is related to anxiety symptoms.
Each item is coded from 0 to 3. The scores for anxiety and depression can therefore vary from 0 to 21, depending on the presence and severity of the symptoms.
A score between 0 and 7 does not indicate the presence of the symptoms of anxiety; a score between 8 and 10 indicates the presence of a moderate symptom; a score of 11 and above indicates a significant number of symptoms of anxiety corresponding to confirmed cases.
|
1 month
|
|
Abdominal circumference
Time Frame: 1 month
|
Using a non-stretch metric tape
|
1 month
|
|
Electrical activity
Time Frame: 1 month
|
Measured using the Megawin ME6000 Electromyograph
|
1 month
|
|
Quality of life for patients with abdominal bloating
Time Frame: 1 month
|
Measured using the Malay version of Bloating Quality of Life (BLQoL-M) Questionnaires.
The responses for BLQoL were in a 7-point Likert scale on different degrees of impact towards individual ranging from 1 = "never/not related to me" to 7 = "always".
Higher scores in BLQoL indicate higher impact towards QoL.
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Vincent Tee, MD, Universiti Sains Malaysia
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 25, 2021
Primary Completion (Actual)
June 28, 2022
Study Completion (Actual)
August 30, 2022
Study Registration Dates
First Submitted
February 25, 2021
First Submitted That Met QC Criteria
March 6, 2021
First Posted (Actual)
March 10, 2021
Study Record Updates
Last Update Posted (Actual)
November 9, 2022
Last Update Submitted That Met QC Criteria
November 4, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- USM/JEPeM/20110562
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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